Laboratory of Neuroendocrinology, Institute of Physiology, Autonomous University of Puebla (BUAP), Puebla, Mexico.
Biochem Biophys Res Commun. 2010 Dec 3;403(1):24-9. doi: 10.1016/j.bbrc.2010.10.100. Epub 2010 Oct 30.
Ghrelin is a multifunctional peptide hormone with roles in growth hormone release, food intake and cell proliferation. With ghrelin now recognized as important in neoplastic processes, the aim of this report is to present findings from a series of in vitro studies evaluating the cellular mechanisms involved in ghrelin regulation of proliferation in the PC-3 human prostate carcinoma cells. The results showed that ghrelin significantly decreased proliferation and induced apoptosis. Consistent with a role in apoptosis, an increase in intracellular free Ca(2+) levels was observed in the ghrelin-treated cells, which was accompanied by up-regulated expression of T-type voltage-gated Ca(2+) channels. Interestingly, T-channel antagonists were able to prevent the effects of ghrelin on cell proliferation. These results suggest that ghrelin inhibits proliferation and may promote apoptosis by regulating T-type Ca(2+) channel expression.
胃饥饿素是一种具有多种功能的肽类激素,在生长激素释放、进食和细胞增殖中发挥作用。由于胃饥饿素在肿瘤发生过程中具有重要作用,本报告的目的是介绍一系列体外研究的结果,这些研究评估了胃饥饿素调节人前列腺癌 PC-3 细胞增殖的细胞机制。结果表明,胃饥饿素显著降低了增殖并诱导了细胞凋亡。与凋亡作用一致,在胃饥饿素处理的细胞中观察到细胞内游离 Ca(2+)水平增加,同时 T 型电压门控 Ca(2+)通道的表达上调。有趣的是,T 型通道拮抗剂能够阻止胃饥饿素对细胞增殖的影响。这些结果表明,胃饥饿素通过调节 T 型 Ca(2+)通道表达来抑制增殖并可能促进细胞凋亡。